Johnson Mahlon, O'Connell Mary, Walter Kevin
Department of Pathology, Division of Neuropathology, University of Rochester, Rochester, NY 14623, USA.
Department of Neurosurgery, University of Rochester, Rochester, NY 14623, USA.
Oncol Lett. 2017 Apr;13(4):2432-2436. doi: 10.3892/ol.2017.5736. Epub 2017 Feb 14.
Several studies have suggested that activation of signal transducer and activator of transcription 3 (STAT3) is associated with initiation, progression and metastasis of numerous types of malignancy. However, the role of the Janus kinase-interleukin 6-STAT3 signaling pathway in the pathogenesis and recurrence of meningiomas is unknown. The present study evaluated STAT3 activation by western blotting and immunohistochemistry and assessed its association with Ki-67 labeling in 13 cases of meningioma in which frozen tissue and ≥5.5-year follow-up information were available, and in formalin-fixed meningioma tissues from 14 cases with an 8.4-year follow-up. The results of the western blot analysis indicated that STAT3 phosphorylation was markedly higher in grade II meningiomas compared with that in grade I, with mean densitometric values of 8.6 and 1.7 following normalization to actin, respectively. High STAT3 phosphorylation/activation was identified in 2 of 3 recurrent World Health Organization (WHO) grade I meningiomas and 0 of 3 non-recurrent meningiomas. Strong STAT3 phosphorylation/activation signal was also found in 2 of 4 recurrent grade II meningiomas and 1 of 3 non-recurrent cases. According to the immunohistochemistry results, phospho-STAT3 was not increased in WHO grade II tumors compared with that in grade I tumors, and was not significantly different between recurrent and non-recurrent cases. Ki-67 labeling was significantly increased in grade II vs. grade I tumors, and was also significantly increased in recurrent compared with non-recurrent grade I meningiomas. The results of the current study suggest that, while detection of phosphorylated/activated STAT3 may be useful in isolated cases, identifying activation may be of little value in predicting recurrence.
多项研究表明,信号转导子和转录激活子3(STAT3)的激活与多种类型恶性肿瘤的发生、发展和转移相关。然而,Janus激酶-白细胞介素6-STAT3信号通路在脑膜瘤发病机制和复发中的作用尚不清楚。本研究通过蛋白质印迹法和免疫组织化学评估了STAT3的激活情况,并在13例有冷冻组织且随访信息≥5.5年的脑膜瘤病例以及14例随访8.4年的福尔马林固定脑膜瘤组织中,评估了其与Ki-67标记的相关性。蛋白质印迹分析结果表明,Ⅱ级脑膜瘤中STAT3磷酸化水平明显高于Ⅰ级,以肌动蛋白标准化后,平均光密度值分别为8.6和1.7。在3例复发性世界卫生组织(WHO)Ⅰ级脑膜瘤中有2例检测到高STAT3磷酸化/激活,3例非复发性脑膜瘤中无此情况。在4例复发性Ⅱ级脑膜瘤中有2例以及3例非复发性病例中有1例也发现了强STAT3磷酸化/激活信号。根据免疫组织化学结果,WHOⅡ级肿瘤中磷酸化STAT3水平与Ⅰ级肿瘤相比并未升高,复发性和非复发性病例之间也无显著差异。Ⅱ级肿瘤与Ⅰ级肿瘤相比,Ki-67标记明显增加,复发性Ⅰ级脑膜瘤与非复发性Ⅰ级脑膜瘤相比,Ki-67标记也明显增加。本研究结果表明,虽然检测磷酸化/激活的STAT3在个别病例中可能有用,但识别其激活情况对预测复发可能价值不大。